Variant #0001037780 (NC_000010.10:g.124810588_124810591del, NM_001609.3:c.1014_1017del (ACADSB))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.124810588_124810591del
DNA change (hg38) -
Published as ACADSB(NM_001609.4):c.1014_1017del (p.(His338Glnfs*11))
ISCN -
DB-ID ACADSB_000039
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADSB NM_001609.3 ?/. - c.1014_1017del r.(?) p.(His338Glnfs*11)


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